POLINEUROMIOPATIA DEL PACIENTE CRITICAMENTE ENFERMO
محفوظ في:
| المؤلف: | |
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| التنسيق: | artículo original |
| الحالة: | Versión publicada |
| تاريخ النشر: | 2011 |
| الوصف: | The critically ill patient’s myopathy is one of the most frequent complications in the intensive care units, it was described for the first time in 1977 by MacFarlane and collaborator. Different names have been used to describe the clinical status that more than a unique entity corresponds to multiple types of muscular damage. Among the most used there are: necrotizing myopathy,quadriplejic myopathy, post-paralysis syndrome and heavy filaments myopathy, although some authors prefer to include these clinical signs under the name of polyneuromyopathy. Nevertheless the most common denomination is acute neuromuscular syndrome. The objective of this document is to analyze the different causes and manifestations of the muscular weakness that critically ill patients develop in the intensive care unit period, and the diagnosis and evaluation of the myopathy of the critically ill patients, taking into account that the most common factors that trigger the development of this entity are: the clinical status, etiopathogenesis in sepsis processes, drug use like the neuromuscular blockaders, corticoids, sedative drugs, the relaxation, the respiratory muscle deficiency and the prolonged stay in bed. |
| البلد: | Portal de Revistas UCR |
| المؤسسة: | Universidad de Costa Rica |
| Repositorio: | Portal de Revistas UCR |
| اللغة: | Español |
| OAI Identifier: | oai:portal.ucr.ac.cr:article/6983 |
| الوصول للمادة أونلاين: | https://revistas.ucr.ac.cr/index.php/clinica/article/view/6983 |
| كلمة مفتاحية: | creatinfosfoquinasa falla multiorgánica alteraciones neuromusculares en pacientes críticamente enfermos neuropatía miopatía polineuropatía |